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61.
详述了国内外最新渣油催化裂化、多产柴油催化裂化、低碳烯烃催化裂化、生产清洁燃料催化裂化及催化剂的技术进展,同时根据我国实际情况对今后催化裂化技术的发展提出了建议。 相似文献
62.
磷铝杂原子固体酸催化剂催化合成乙酸异丙酯 总被引:5,自引:0,他引:5
高文艺 《精细石油化工进展》2003,4(12):30-31
以丙烯和乙酸为原料 ,自制的磷铝杂原子固体酸作催化剂催化合成了乙酸异丙酯 ,考察了反应温度、反应压力、反应空速 (LHSV)及催化剂用量对酯化反应的影响 ,同时考察了固体酸催化剂的重复使用性。确定了最佳合成条件 :反应压力 1 5MPa,反应温度 1 60℃ ,反应空速2 0h-1,催化剂用量 2 0g。在此条件下 ,酯化率可达 91 5 % ,乙酸异丙酯选择性达 99 0 % ,且催化剂的重复使用性良好。 相似文献
63.
合成直链烷基苯环境友好固体酸催化剂的研究 Ⅲ .催化剂失活原因分析 总被引:1,自引:0,他引:1
采用固定床反应器,对催化剂的稳定性进行了初步评价。在120℃、空速相同、液固反应条件下,高苯烯比时催化剂的稳定性明显高于低苯烯比时;在苯烯比和空速相同、液固反应条件下,相对低温反应时,催化剂的稳定性明显高于高温反应。IR分析结果表明,同新鲜和反应后未失活的催化剂相比,失活后催化剂的活性组分特征衍射峰消失,出现的新的特征衍射峰可能同—CH基的振动有关。TG分析结果表明,失活后催化剂在空气流中焙烧,失重幅度比新鲜催化剂大。 相似文献
64.
65.
On the basis of new concept using a solid disperse phase we have developed an efficient catalytic solid-phase-system for epoxidations of alkenes using urea–hydrogen peroxide (urea–H2O2) complex and cetylpyridinium dodecatungstate ((CetylPy)10[H2W12O42]) catalyst on fluorapatite (FAp). The recovered solid catalyst phase was reused to keep the catalytic activity after several times. In the conceptual idea it is a key point that in situ solid-phase-activation of the catalyst with urea–H2O2 proceeds to form microcrystals of the active species dispersed on the solid phase. The dispersion of the catalyst on FAp in the case of tungstic acid (H2WO4) was suggested by EPMA analysis. We proposed the peroxo type of species keeping the parent polyoxometalate framework as novel active species from FT-IR spectroscopic studies. FAp phase plays important roles of dispersing the active species on its surface to have high catalytic activity and of stabilizing the active species to lead to high reusability. 相似文献
66.
67.
A solid oxide fuel cell using a thin ceria-based electrolyte film with a Ru-catalyzed anode was directly operated on hydrocarbons, including methane, ethane, and propane, at 600 °C. The role of the Ru catalyst in the anode reaction was to promote the reforming reaction of the unreacted hydrocarbons by the produced steam and CO2, which avoided interference from steam and CO2 in the gas-phase diffusion of the fuels. The resulting peak power density reached 750 mW cm−2 with dry methane, which was comparable to the peak power density of 769 mW cm−2 with wet (2.9 vol.% H2O) hydrogen. More important was the fact that the cell performance was maintained at a high level regardless of the change in the methane utilization from 12 to 46% but was significantly reduced by increasing the hydrogen utilization from 13 to 42%. While the anodic reaction of hydrogen was controlled by the slow gas diffusion, the anodic reaction of methane was not subject to the onset of such a gas-diffusion process. 相似文献
68.
K. Y. Cheah T. S. Tang Fujio Mizukami Shu-ichi Niwa Makoto Toba Y. M. Choo 《Journal of the American Oil Chemists' Society》1992,69(5):410-416
A new catalyst, ruthenium-tin-alumina is found to selectively hydrogenate oleic acid to 9-octadecen-1-ol (oleyl + elaidyl
alcohol) at low pressure with high yield. Catalyst preparation methods, catalyst raw materials and activation conditions have
a significant effect on the activity of the catalyst. The optimum atomic ratio of ruthenium to tin is about 1:2. Catalyst
prepared by an improved sol-gel method shows higher activity and selectivity than catalysts prepared by impregnation and coprecipitation
methods. Chloride is found to have a negative effect on catalytic activity. The best catalyst is prepared from chloride-free
ruthenium and tin raw materials. Under the optimum reaction conditions of 250°C and 5.6 MPa, the selectivities for 9-octadecen-1-ol
and total alcohol (9-octadecen-1-ol + stearyl alcohol) formation are 80.9% and 97%, respectively, at a conversion of 81.3%. 相似文献
69.
P. S. Lawson 《Biomass & bioenergy》1992,2(1-6):319-330
In recent years it has been recognised by an increasing number of nations that there is considerable energy potential within MSW. As a result many countries have established R,D& D programmes to examine methods of exploiting this potential. The IEA's MSW Conversion Activity was set up in 1986 to provide an infrastructure for sharing information and co-ordinating work in this area internationally. This Activity was extended in 1989 and currently a total of 9 nations participate in it.
To cope with the wide scope of the area (encompassing both biological and thermal processing of MSW) the Activity was divided into three subgroups or Expert Working Groups (EWGs). Each of these dealt with a distinct area of expertise:
- 1. •Downstream effects of source separation and screening of MSW
- 2. •Sampling and analytical protocols
- 3. •Landfill gas
In addition to these groups a central secretariat based at Harwell (UK) has provided guidance, established and administered databases of contacts and produced a series of national reports.
This paper describes the achievements of the Activity and discusses work proposed for the future. 相似文献
70.
Properties and Performance of Cation-Doped Ceria Electrolyte Materials in Solid Oxide Fuel Cell Applications 总被引:1,自引:0,他引:1
Christopher Milliken Sivaraman Guruswamy Ashok Khandkar 《Journal of the American Ceramic Society》2002,85(10):2479-2486
Cation-doped CeO2 electrolyte has been evaluated in single-cell and short-stack tests in solid oxide fuel cell environments and applications. These results, along with conductivity measurements, indicate that an ionic transference number of ∼0.75 can be expected at 800°C. Single cells have shown a power density >350 mW/cm2 . Multicell stacks have demonstrated a peak performance of >100 mW/cm2 at 700°C using metallic separators. 相似文献